Clinical Trials Directory

Trials / Completed

CompletedNCT02748876

Effect of His-Ventricular (HV) Interval Optimisation in Cardiac Resynchronisation Therapy

A Randomised Cross-over Pilot Study of the Effect of His-Ventricular (HV) Interval Optimisation in Cardiac Resynchronisation Therapy

Status
Completed
Phase
N/A
Study type
Interventional
Enrollment
14 (actual)
Sponsor
Hull University Teaching Hospitals NHS Trust · Other Government
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

Cardiac resynchronisation therapy (CRT) is a specialised type of pacemaker used in patients with severe heart failure to improve symptoms and survival. Approximately one third of patients treated with CRT do not notice significant improvement in their symptoms and this may be due to inadequate co-ordination between the upper and lower chambers of the heart (atrioventricular dyssynchrony). The investigators propose a new method to achieve atrioventricular synchrony in CRT based on measurements of electrical conduction from within the heart. Patients referred for CRT implantation at Castle Hill Hospital are eligible to participate. During CRT implantation, additional measurements, will be recorded from within the heart. After implantation, device settings will be adjusted to either standard or electrophysiologically-optimised settings with cross-over at 4 months. The investigators hypothesis is that patients with optimised settings will derive additional benefit compared to patients with standard pacemaker-determined settings.

Conditions

Interventions

TypeNameDescription
OTHERHis-Ventricular (HV) optimisationOptimisation of atrioventricular pacing interval

Timeline

Start date
2016-09-29
Primary completion
2017-04-28
Completion
2018-03-15
First posted
2016-04-22
Last updated
2019-07-17

Locations

1 site across 1 country: United Kingdom

Source: ClinicalTrials.gov record NCT02748876. Inclusion in this directory is not an endorsement.